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dysgerminoma/bolest břicha
Odkaz je uložen do schránky
Strana 1 z 47 Výsledek
Advanced ovarian dysgerminoma infiltrating both ovaries and uterus in a 7-year-old girl.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Introduction. Ovarian dysgerminoma is a rare malignant ovarian germ cell tumor with its peak incidence in young women. Abdominal pain, abdominal distention, and the presence of a palpable mass are common symptoms at presentation. Depending on the FIGO stage at presentation the prognosis of
Surgical resection of a dysgerminoma in a mare.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
A mare was referred for further evaluation of a mass found in the left caudal abdomen during a routine postpartum reproductive palpation. The mare was clinically normal with no history of health problems. Ultrasonographic examination of the mass confirmed its presence, but the origin of the mass
Torsion of Ovarian Dysgerminoma in a Child: Role of Computed Tomography.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Dysgerminomas are malignant germ cell tumors of the ovary that most commonly occur in the adolescent population. Ovarian dysgerminoma presenting with complications like torsion is a rare entity in the pediatric age group. Cross-sectional imaging plays a crucial role in diagnosis, tumor staging
[Clinical analysis of 57 patients with ovarian dysgerminoma].
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
OBJECTIVE
Ovarian dysgerminoma is an uncommen ovarian malignancy. Its clinical features are special and there are many factors influencing the prognosis. If treated properly, the patient can be cured. Otherwise it may endanger the patient's life. The aim of this study is to investigate the clinical
[Antierythrocyte antibodies due to ovarian dysgerminoma. A case report].
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The case of a 24-year-old woman with fever, abdominal pain and weight loss, is presented. Right ovarian dysgerminoma was diagnosed; group A blood, negative direct Coombs. The search for free serum antibodies was positive, with specificity: auto anti 1, anti P with activity at 37 degrees C.
[A case of PEP(BEP)-resistant ovarian dysgerminoma successfully treated by VeIP therapy].
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Ovarian germ cell tumors are malignant tumors which commonly develop during childhood, and which are sensitive to chemotherapy. We have had a case of germ cell tumors which showed resistance to first-line PEP(BEP)chemotherapy. As second-line chemotherapy, VeIP therapy was used, because it is
Bilateral Gonadoblastoma With Dysgerminoma in a Phenotypically Normal Female With 46XX Karyotype: Report of a Rare Case and Literature Review
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Gonadoblastoma is a rare ovarian neoplasm which belongs to "germ cell-sex cord-stromal tumor" category. This tumor is frequently associated with invasive germ cell malignancy. It commonly arises in dysgenetic gonads of young individuals who are phenotypically females but possess 46XY karyotype. It
Internal hemorrhage caused by a twisted malignant ovarian dysgerminoma: ultrasonographic findings of a rare case and review of the literature.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
OBJECTIVE
Ovarian cancer presents as an acute abdomen very rarely. The purpose of the study is the description of a right ovarian malignant dysgerminoma presenting as an abdominal emergency.
METHODS
A 16-year-old white female presented with acute abdominal pain in the right iliac fossa. On physical
[An ovarian tumor with structural gonadoblastoma, dysgerminoma and choriocarcinoma].
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
A 14 1/2-year old girl with menometrorrhagia followed by amenorrhea and abdominal pain had a pelvic resistance with limited mobility. Histology of a left ovarian tumour showed gonadoblastoma turning to dysgerminoma and associated with choriocarcinoma (M-9073/1, M-9060/3, M-90101/3). Genuine ovarian
Ovarian dysgerminoma in an adolescent: a case report.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND
Ovarian cancer is the second most frequent gynaecological cancer in Nigeria ranking next after carcinoma of the cervix. It has the highest case-fatality rate worldwide because of insidious onset, lack of effective screening methods and late presentation. This case of a sixteen-year old
Ovarian dysgerminoma and acute abdomen.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND
Ovarian dysgerminoma cases are very rarely presented together with acute abdomen. The purpose of this study is to present dysgerminoma ovarii with abdominal pain in lower right abdominal part after abdominal trauma as an abdominal emergency.
METHODS
Our 12-year old female patient was
Imaging Findings in Dysgerminoma in a Case of 46 XY, Complete Gonadal Dysgenesis (Swyer syndrome).
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
A 46 XY pure gonadal dysgenesis also known as Swyer syndrome. These patients are phenotypic females with normal female external genitalia and absent testicular tissue. The patients with swyer syndrome have streak gonads and increased risk of dysgerminoma and gonadoblastoma. We present a case of
Paraneoplastic Cholestasis Associated With Ovarian Dysgerminoma.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND
Paraneoplastic syndromes are disorders caused by cancer that are not a direct result of the cancer mass itself or metastases to the affected organ. Paraneoplastic cholestasis is described with lymphoma and renal cell carcinoma. Unlike ovarian carcinoma, paraneoplastic syndromes are rarely
Ovarian dysgerminoma with normal serum tumour markers presenting in a child with precocious puberty.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
A 7-year-old female child was presented to the emergency room with acute abdominal pain and vaginal bleeding. Her assessment revealed a firm large lower abdominal mass with evidence of precocious puberty with bilaterally symmetrically enlarged breast (Tanner stage B4-P1-A1). Abdominal imaging showed
Fine needle aspiration diagnosis of bilateral dysgerminoma with syncytiotrophoblastic giant cells.
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Dysgerminoma accounts for only 1-3% of ovarian cancers and about 30-40% of all ovarian germ cell malignant tumors. Literature states that about 2% of nonpregnant patients with dysgerminomas present with elevated serum or urine levels of human chorionic gonadotropin (hCG). Here, we report a 34
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